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89466-42-2

4-Chloro-6-methoxy-2-(methylthio)pyrimidine

Catalog#: AR00GWLE  |   CAS#: 89466-42-2  |   MDL#: MFCD10574952  |   MF: C6H7ClN2OS  |   MW: 190.6506

Packsize Purity Price Availability Quantity
100mg 95% $5.00 Global Stock Buy Now Add To Cart
250mg 95% $7.00 Global Stock Buy Now Add To Cart
1g 95% $19.00 Global Stock Buy Now Add To Cart
5g 95% $69.00 Global Stock Buy Now Add To Cart
10g 95% $111.00 Global Stock Buy Now Add To Cart
25g 95% $225.00 Global Stock Buy Now Add To Cart
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Catalog Number AR00GWLE
Chemical Name 4-Chloro-6-methoxy-2-(methylthio)pyrimidine
CAS Number 89466-42-2
Molecular Formula C6H7ClN2OS
Molecular Weight 190.6506
MDL Number MFCD10574952
SMILES COc1cc(Cl)nc(n1)SC

4-Chloro-6-methoxy-2-(methylthio)pyrimidine is a versatile compound frequently employed in chemical synthesis for its unique reactivity and functional group compatibility. Its application in organic synthesis extends to various industries, including pharmaceuticals, agrochemicals, and materials science. This compound serves as a key intermediate in the construction of complex molecules due to its ability to participate in a range of chemical reactions. Its chloro and methoxy substituents provide opportunities for selective modification, making it a valuable building block in the creation of target molecules with specific properties. Additionally, the presence of the methylthio group enhances its reactivity profile, allowing for diverse transformation pathways in synthesis.In pharmaceutical chemistry, 4-Chloro-6-methoxy-2-(methylthio)pyrimidine is utilized for the synthesis of novel drug candidates and pharmaceutical intermediates. Its structural features make it particularly useful in medicinal chemistry efforts aimed at developing bioactive compounds with potential therapeutic applications. By incorporating this compound into synthetic routes, chemists can access a broad spectrum of structurally diverse compounds for biological testing and drug discovery.In agrochemical research, this pyrimidine derivative plays a crucial role in the preparation of active ingredients for crop protection products. Its compatibility with various functional groups enables the construction of pesticide and herbicide compounds with improved efficacy and selectivity. The introduction of the methylthio group can further enhance the biological activity of these agrochemicals, offering new solutions for pest and weed control in agriculture.Moreover, in materials science, 4-Chloro-6-methoxy-2-(methylthio)pyrimidine contributes to the synthesis of advanced materials with tailored properties. By exploiting its reactivity in polymerization and other material synthesis processes, researchers can design polymers, coatings, and additives with specific functionalities and characteristics. This compound's versatility and synthetic accessibility make it a valuable tool for developing innovative materials for a wide range of applications.
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